Coupling In nanoclusters and Bi nanoparticles in nitrogen-doped carbon for enhanced CO2 electroreduction to HCOOH

被引:0
|
作者
Hu, Yanna [1 ]
Cao, Xian [2 ,3 ]
Zhang, Kai [2 ,3 ]
Chen, Shichao [1 ]
Wei, Lingzhi [1 ]
Ye, Chun [2 ,3 ]
Pan, Guoxing [1 ]
Hu, Lin [1 ,2 ,3 ]
机构
[1] Anhui Univ, Inst Phys Sci & Informat Technol, Hefei 230601, Anhui, Peoples R China
[2] Chinese Acad Sci, Anhui Key Lab Low Energy Quantum Mat & Devices, High Magnet Field Lab, HFIPS, Hefei 230031, Anhui, Peoples R China
[3] Univ Sci & Technol China, Hefei 230026, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
In nanoclusters; Bi nanoparticles; Synergistic effects; High selectivity toward HCOOH; Stability; Electrochemical CO2 reduction; ELECTROCHEMICAL REDUCTION; FORMATE; NANOSHEETS;
D O I
10.1016/j.jelechem.2024.118711
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
CO2 2 electrochemical reduction reaction (CO2RR) 2 RR) to formic acid (HCOOH) is beneficial for the recycling of carbon resources, which needs the highly selective catalysts with long-term stability for HCOOH production. In this study, the coupling of In nanoclusters (Inclus) clus ) and Bi nanoparticles (Binps) nps ) in nitrogen-doped carbon was designed by the thermal decomposition of the mixture of bimetallic MOFs and dicyanamide. When the In/Bi molar ratio was 1:2 (Inclus/Binps-1:2), clus /Bi nps-1:2), the hybrid catalyst achieved a HCOOH Faradaic efficiency (FE HCOOH ) of 94.5 % at-1.1 V vs reversible hydrogen electrode (RHE) in an H-type electrolysis cell, superior to that of single metal counterparts. Moreover, the Inclus/Binps-1:2 clus /Bi nps-1:2 can maintain high stability of structures during the catalytic process, leading to no significant decay of FE HCOOH over 32 h. The enhanced performance of Inclus/Binps-1:2 clus /Bi nps-1:2 is attributed to the strong electron interactions induced by the charge transfer between the In and Bi sites in Inclus/Binps-1:2 clus /Bi nps- 1: 2 catalyst. The tuned electronic structure results in an offset effect that optimizes the binding energy to HCOO* intermediate, thus accelerating the CO2 2 to HCOOH conversion, as proven by the in-situ ATR-SEIRAS and density functional theory (DFT) calculations.
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页数:8
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